Different Therapeutical Modalities Associated to Hamstring Flexibility Training

Not Applicable

Completed

• Conditions: Range of Motion, Articular

• Registration Number: NCT03021850
• Lead Sponsor: Federal University of Health Science of Porto Alegre

Brief Summary

The purpose of this study is to compare the acute effect of the use of different thermal modalities associated to the training of passive flexibility of the hamstring muscles in the amplitude of motion of the knee extension.

Detailed Description

Context: In the literature there is a disagreement of results and protocols regarding the use of thermal modalities associated with the training of flexibility of the hamstring muscles. Most studies on the subject, used the heat and cryotherapy prior to stretching these. Therefore, the investigators aimed to conduct an experimental study using the therapeutics term concomitant arrangements to passive static stretching these muscles.

Methods: Clinical trial randomized crossover, which will a sample of 42 subjects (healthy young men, aged 20 to 30 years). Were divided into 3 groups (Group 1 passive static stretching hamstrings, Group 2 heat + passive static stretching hamstrings and Group 3 cryotherapy + static stretching hamstrings passive) with 14 subjects each. Where the participants will control themselves, since all carry out the three interventions, only at different times. Each action will be performed every 7 days. Individuals will be subjected to active test of the range of motion of knee extension (goniometer) and hamstring muscle strength (dynamometer).

Study Timeline

• Study Start: 2016-04-02
• Study First Submitted: 2017-01-06
• Study First Submitted QC: 2017-01-12
• Study First Posted: 2017-01-16
• Primary Completion: 2017-02-10
• Study Completion: 2017-07-06
• Status Verified: 2017-10
• Last Update Submitted: 2017-10-17
• Last Update Posted: 2017-10-18

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Male
• Target Recruitment: 34

Inclusion Criteria

• Healthy men with knee extension range less than or equal to 160 degrees.

Exclusion Criteria

• Have exercised in the last 48 hours before the intervention session;
• Previous neurological, muscular or articular disease that influences the performance of the training;
• Anterior lower limb surgery;
• Presence of painful symptoms or edema in the lower limbs;
• Hypersensitivity to ice or heat;
• Raynaud's syndrome;
• Loss of local thermal sensitivity;
• Have metallic implants;
• Use of cardiac pacemaker;
• Presence of malignant tumor;
• Arterial diseases;
• Deep venous thrombosis or phlebitis;
• Fever and inflammatory processes;
• Bleeding processes;
• Osteomyelitis;
• Epilepsy;
• Pulmonary and bone tuberculosis;
• Kidney or urinary tract infection;
• Cryoglobulinemia;

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: CROSSOVER

Primary Outcome Measures

Name	Time	Method
Change of Active Knee Extension Test	3 weeks	Active Knee Extension Test is performed in a standardised procedure and is measured in degrees.

Secondary Outcome Measures

Name	Time	Method
Change of Peak Torque of flexors and knee extensors	3 weeks	Peak torque of flexors and knee extensors is performed in an isokinetic dynamometer (Biodex system III), in a standardised procedure.
Change of Passive Resistance flexors and knee extensors	3 weeks	Passive Resistance of flexors and knee extensors is performed in an isokinetic dynamometer (Biodex system III), in a standardised procedure.

Trial Locations

Locations (1)

Federal University of Health Science of Porto Alegre; 🇧🇷 Porto Alegre, Rio Grande do Sul, Brazil